High throughput screening by multichannel glass fiber fluorimetry

被引:11
作者
Schober, A
Gunther, R
Tangen, U
Goldmann, G
Ederhof, T
Koltermann, A
Wienecke, A
Schwienhorst, A
Eigen, M
机构
[1] EVOTEC,D-22529 HAMBURG,GERMANY
[2] MAX PLANCK INST BIOPHYS CHEM,D-37018 GOTTINGEN,GERMANY
关键词
D O I
10.1063/1.1148110
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
As a tool for screening large numbers of biological samples by means of amplification (e.g., Q beta or PCR) we have constructed a thermocycler that includes optionally a 96-channel or 960-channel glass fiber fluorimeter (combined with a cooled charge-coupled-device camera). We briefly describe the system integration of all components like liquid handling, thermostats, an x,y,z robot arm, and the glass fiber fluorimeter. The integrated glass fiber fluorimeter allows sensitive on-line measurements in 960 channels within 5 s. Two different screening procedures were carried out. In a first experiment PCR reactions were done in the presence of the known PCR inhibitor hematin and its suppressor transferrin. The system was used to titrate the suppressor with the inhibitor hematin in order to determine the maximum inhibitor concentration tolerated at a given suppressor concentration. We processed 96 PCR samples in parallel with 11 different concentration steps. In a second experiment the 960-channel glass fiber fluorimeter was used to monitor on line the amplification of the Q beta system in the presence or absence of an inhibitor (heparin). Since the doubling time of Q beta RNA variants is about 20 s, on-line detection is crucial for the experimental setup. The evolution of new RNA species adapted to high inhibitor concentrations could be proved by comparison of the fluorimetric signal and electrophoresis. (C) 1997 American Institute of Physics.
引用
收藏
页码:2187 / 2194
页数:8
相关论文
共 57 条
[1]   TIME-RESOLVED FLUORESCENCE SPECTROSCOPY AND INTRACELLULAR IMAGING OF DISULFONATED ALUMINUM PHTHALOCYANINE [J].
AMBROZ, M ;
MACROBERT, AJ ;
MORGAN, J ;
RUMBLES, G ;
FOLEY, MSC ;
PHILIPS, D .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 1994, 22 (02) :105-117
[2]   FLUORESCENCE DIGITAL IMAGING MICROSCOPY IN CELL BIOLOGY [J].
ARNDTJOVIN, DJ ;
ROBERTNICOUD, M ;
KAUFMAN, SJ ;
JOVIN, TM .
SCIENCE, 1985, 230 (4723) :247-256
[3]  
BALALRD DH, 1982, COMPUTER VISION
[4]  
BARTEL DP, 1993, SCIENCE, V261, P411
[5]  
BEAUDRY AA, 1992, SCIENCE, V257, P63
[6]   INVITRO SELECTION OF ACTIVE HAIRPIN RIBOZYMES BY SEQUENTIAL RNA-CATALYZED CLEAVAGE AND LIGATION REACTIONS [J].
BERZALHERRANZ, A ;
JOSEPH, S ;
BURKE, JM .
GENES & DEVELOPMENT, 1992, 6 (01) :129-134
[7]   APPLICATIONS OF A SLOW-SCAN CCD CAMERA IN PROTEIN ELECTRON CRYSTALLOGRAPHY [J].
BRINK, J ;
CHIU, W .
JOURNAL OF STRUCTURAL BIOLOGY, 1994, 113 (01) :23-34
[8]   64-CHANNEL FIBER OPTIC SPECTROMETER FOR A DUAL-WAVELENGTH INTERFEROMETRIC PRESSURE SENSOR ARRAY [J].
CASTRACANE, J ;
CLOW, LP ;
WEGENER, S ;
SEIDLER, G .
REVIEW OF SCIENTIFIC INSTRUMENTS, 1995, 66 (06) :3668-3671
[9]   IMAGING APPLICATIONS FOR CHEMICAL-ANALYSIS UTILIZING CHARGE-COUPLED-DEVICE ARRAY DETECTORS [J].
EARLE, CW ;
BAKER, ME ;
DENTON, MB ;
POMEROY, RS .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 1993, 12 (10) :395-403
[10]  
EIGEN M, 1986, CHEM SCRIPTA, V26B, P13